A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029350



Internal ID19118569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163318463..163379819hg38UCSC Ensembl
Innerchr5:162745469..162806825hg19UCSC Ensembl
Innerchr5:162678047..162739403hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3861357
hg1961357
hg1861357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5826n100
Supporting Variantsnssv3648237, nssv3648239, nssv3648238, nssv3746663
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029350
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer